DURADRY AM- aluminum zirconium trichlorohydrex glycine stick

DURADRY AM by

Drug Labeling and Warnings

DURADRY AM by is a Otc medication manufactured, distributed, or labeled by Novadore USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum Zirconium Trichlorohydrex Glycine 20%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

Warnings

For external use only
Stop use if rash or irritation occurs.

Do not use

• On broken skin.

Ask a doctor before use

if you have kidney disease

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply to underarms only.

Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Dimethicone, Zinc Ricinoleate, Petrolatum, Aluminum Starch Octenylsuccinate Fragrance.

Questions?

Visit us at www.duradry.com/am

Designed & developed by:
NOVADORE USA, INC
Miami, FL

DURADRY AM (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINE)

INGREDIENTS AND APPEARANCE

DURADRY AM 
aluminum zirconium trichlorohydrex glycine stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69990-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH)	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
DIMETHICONE (UNII: 92RU3N3Y1O)
ZINC RICINOLEATE (UNII: BOH1Z111J2)
PETROLATUM (UNII: 4T6H12BN9U)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69990-200-01	1 in 1 CARTON	01/01/2015
1		65 g in 1 CYLINDER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/01/2015

Labeler - Novadore USA, LLC (079777451)

Registrant - Novadore USA, LLC (079777451)

Establishment
Name	Address	ID/FEI	Business Operations
Novadore USA, LLC		079777451	label(69990-200)

Establishment
Name	Address	ID/FEI	Business Operations
VVF Kansas Services LLC		833164242	manufacture(69990-200)